Package 16714-632-01
Brand: alendronate sodium
Generic: alendronate sodiumPackage Facts
Identity
Package NDC
16714-632-01
Digits Only
1671463201
Product NDC
16714-632
Description
1 BLISTER PACK in 1 CARTON (16714-632-01) / 4 TABLET in 1 BLISTER PACK
Marketing
Marketing Status
Brand
alendronate sodium
Generic
alendronate sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fed80488-a7dd-4a81-b79a-75f10e71fa8e", "openfda": {"upc": ["0316714631011", "0316714631110"], "unii": ["2UY4M2U3RA"], "rxcui": ["904396", "904419", "904431"], "spl_set_id": ["4323d3aa-cbb0-41e2-aba7-7a94a0516993"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (16714-632-01) / 4 TABLET in 1 BLISTER PACK", "package_ndc": "16714-632-01", "marketing_start_date": "20080804"}, {"sample": false, "description": "5 BLISTER PACK in 1 CARTON (16714-632-02) / 4 TABLET in 1 BLISTER PACK", "package_ndc": "16714-632-02", "marketing_start_date": "20080804"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (16714-632-11) / 10 TABLET in 1 BLISTER PACK (16714-632-10)", "package_ndc": "16714-632-11", "marketing_start_date": "20080804"}], "brand_name": "Alendronate Sodium", "product_id": "16714-632_fed80488-a7dd-4a81-b79a-75f10e71fa8e", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "16714-632", "generic_name": "Alendronate Sodium", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alendronate Sodium", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "35 mg/1"}], "application_number": "ANDA090124", "marketing_category": "ANDA", "marketing_start_date": "20080804", "listing_expiration_date": "20261231"}